BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to a method and apparatus for producing a pattern member
used as an electron display material such as color filters, organic EL (electroluminescence)
and the like, and a pattern member thus produced. Here, the pattern member includes
films and sheets of color filters and organic displays, and also includes transfer
films and sheets for producing the above-mentioned color filters and organic displays.
Description of the Related Art
[0002] Conventionally used as an electron display material such as LCD color filters, organic
EL pixels and the like are pattern members having a micron order fine pattern in the
form of stripe or matrix of single color or three colors such as, for example, R (red),
G (green), B (blue) and the like formed on a glass substrate, sheet substrate, film
and the like.
[0003] As the method of producing such a pattern member, methods as shown below have been
suggested until now (those regarding color filter production methods are mainly listed).
1) Relief dyeing method: The surface of a substrate such as a sheet and the like is
patterned into given form using a photosensitive resist, then, the sheet is immersed
in a dyeing solution to be colored (for each of RGB, three times in total).
2) Pigment dispersing method: A photosensitive resist containing a dispersed pigment
is applied on the surface of a substrate, and exposed and developed to form a pattern
(for each of RGB, three times in total).
3) Vacuum deposition method: Coloring material particles are heated to be evaporated,
and adhered to the masked surface of a sheet to form a pattern (for each of RGB, three
times in total).
4) Inkjet method: Coloring inks of RGB three colors are sprayed in small amount at
given position by an inkjet method to effect patterning.
5) Electrodeposition method: A transparent electrode is patterned in given form, and
electrodeposition is repeated three times on this, to make a colored pattern.
6) Offset printing method: Ink containing a dispersed pigment is printed three times
on the surface of a sheet by an offset printing method.
[0004] However, these methods have the following problems and none of them is admitted as
a satisfactory production method.
1. A relief dyeing method, pigment dispersing method and electrodeposition method
include a lot of processes and are not suitable for mass production.
2. With a vacuum deposition method, it is difficult to produce a pattern member of
large area.
3. A vacuum deposition method needs large equipment cost.
4. In all of the above-mentioned six methods, it is necessary to add special chemicals
such as a hardening resin and the like to ink, and development of recipe is necessary,
and additionally, an influence exerted on the ability of an electron display by the
special chemicals is worried.
5. With the inkjet method and offset printing method, it is difficult to obtain an
ink layer having constant thickness.
6. With the offset printing method, it is difficult to keep high accuracy of positioning
in forming patterns of respective colors.
[0005] A production method satisfactory particularly in the following points, among the
above-mentioned problems, is desired. Namely, a first point is mass production by
a cheap equipment with a small number of processes, and a second point is large degree
of freedom in ink selection and no necessity to add special chemicals to ink.
[0006] As the production method approximately satisfying such conditions, Japanese Patent
Application Laid-Open (JP-A) No. 9-90117 discloses a method in which, in forming three
kinds of colored layers in given pattern on a sheet, unnecessary portions of a colored
solidified film are removed by transferring from a dry film having a colored solidified
film made of a resin composition containing a dispersed coloring material to an intaglio
surface having a given pattern, then, the colored solidified film of given pattern
remaining on the dry film is transferred onto a sheet, for each color.
[0007] However, this production method needs two processes: a process in which, after production
of a dry film, further, unnecessary portions of a colored solidified film on a dry
film are removed for each color, and a process in which a colored solidified film
remaining on a dry film is transferred onto a sheet, and it is difficult to decrease
production cost.
[0008] For solving the above-mentioned problems 1 to 6, JP-A No. 11-260549 discloses a pattern
member production method in which "A light-heat conversion layer and a heat propagation
layer are formed on a film, and on this is formed a cathode layer, then, a light-emitting
layer is formed in superposition, further, a hole injectable adhesive layer is formed
in superposition, then, the film-formed side of a film is pasted on a substrate having
a stripe patterned ITO anode, then, the film rear surface side is irradiated by YAG
laser selectively so as to form a cathode shape, to transfer the multiply-formed layers
onto a substrate. Then, the film is removed, driving means is connected to the substrate
onto which the multiply-formed layers have been transferred, and a sealing treatment
is performed to obtain an organic EL display."
[0009] This pattern member production method of transfer mode is a dry process, therefore,
damages by an organic solvent, water and the like are not given to an organic material
constituting an organic electroluminescence element, and a highly precise pattern
can be formed.
[0010] However, this transfer mode has the following problem. Namely, in this transfer mode,
a transfer substrate and a supporting substrate for an organic electroluminescence
element have to be closely adhered completely, at parts intended to be transferred,
in the transferring operation, however, irregularity by a pattern-formed electrode
layer, an organic material layer and the like are present on the surface of the supporting
substrate, namely, this surface is not completely flat, consequently, a gap may be
formed between the transfer substrate and the organic electroluminescence element,
and transfer is not performed at a such gap part, resultantly, short-circuit between
electrodes occurs at this part, causing a display defect and yield decrease.
[0011] For solving this problem, JP-A No. 2001-196168 discloses "A method of producing an
organic electroluminescence element, comprising a process in which at least a first
electrode layer is firmed on a supporting substrate, a process in which a material
constituting an electroluminescence layer and/or a second electrode layer is formed
as a transfer layer on a transfer substrate, a process in which the first electrode
layer-formed surface of the supporting substrate and the transfer layer-formed surface
on the transfer substrate are crimped by a crimping roller, and a process in which
the transfer layer formed on the transfer substrate is transferred onto the first
electrode layer-formed surface side of the supporting substrate."
[0012] However, since this method disclosed in JP-A No. 2001-196168 is a method in which,
in producing a multi-color pattern member, a difference is made in film thickness
of transfer layers of respective colors formed on a color transfer substrate of a
plurality of colors, and transfer layers are transferred sequentially onto the supporting
substrate based on the difference in film thickness, to form a multi-color pattern,
there is a problem that control of the film thickness of a transfer layer is difficult,
and if the difference in film thickness is not controlled to a given value, correct
transfer cannot be conducted.
SUMMARY OF THE INVENTION
[0013] In view of the above-mentioned conditions, the object of the present invention is
to provide a method and apparatus for producing a pattern member at high productivity
and low cost, and a pattern member thus produced.
[0014] The first production method of the methods of producing a pattern member according
to the present invention for attaining the above-mentioned object comprises:
by applying a color ink on each of a plurality of films and drying the color ink,
producing a plurality of single color films each having a different color of a plurality
of colors and a color ink layer formed on a surface of each single color film; and
transferring a part of a color ink layer to a substrate to produce a pattern member
having a multi-color pattern made of color inks of the plurality of colors formed
on the substrate by repeating, at frequency corresponding to the number of the plurality
of colors, an operation of overlapping one of the plurality of single color films
having one color on the substrate such that a color ink layer of the single color
film comes in contact with the substrate, and then, pressing the overlapped substrate
and single color film by a pressing member having a convex portion of given pattern
formed on its surface, to transfer a portion of the color ink layer corresponding
to a pattern of the convex portion to the substrate.
[0015] According to the first method of producing a pattern member of the present invention,
after production of a single color film corresponding to the dry film referred in
the above-mentioned conventional example, a pattern member is produced only in the
above-mentioned step of transferring a part of a color ink layer to a substrate transfer.
According to the method of producing a pattern member of the present invention, a
pattern member can be produced with a small number of processes, namely, at high productivity
and low cost.
[0016] Here, the step of transferring a part of a color ink layer to a substrate includes
a process of applying an ink of given color on the substrate by any application means
selected from a die coater, bar coater, spin coater and gravure coater.
[0017] In the first method of producing a pattern member of the present invention, a multi-color
pattern sheet can be produced at low cost by any of these application process.
[0018] The step of transferring a part of a color ink layer to a substrate may be a step
in which transfer is conducted using a pressing member having a convex portion of
a pattern in the form of stripe or matrix formed on its surface.
[0019] In the first method of producing a pattern member of the present invention, a pattern
member of any of the above-mentioned forms can be produced at low cost.
[0020] For attaining the above-mentioned object, the present invention also provides an
apparatus of producing a pattern member that has a multi-color pattern made of color
inks of a plurality of colors on its surface by repeating, at frequency corresponding
to the number of the plurality of colors, an operation of overlapping on a given substrate
a plurality of single color films each having a different color of the plurality of
colors and a color ink layer formed on its surface, to transfer the color ink layer
on the single color film to the substrate, the apparatus comprising:
transferring means corresponding to the number of the plurality of colors, transferring
the color ink layer of the single color film to the substrate, the transferring means
being constituted of a patterning roll having a convex portion of given pattern formed
on its surface and a facing roll placed facing the patterning roll so that the patterning
roll and facing roll sandwich both the substrate and the single color film between
them;
substrate feeding means sequentially feeding the substrate to the transfer corresponding
to the number of the plurality of colors; and
single color film feeding means corresponding to the number of the plurality of colors,
feeding a single color film of one color among the single color films of the plurality
of colors, between the patterning roll and the substrate fed to a nip portion sandwiched
by the patterning roll and the facing roll, such that the color ink layer of the single
color film overlaps on and comes in contact with the substrate.
[0021] The apparatus of producing a pattern member of the present invention, by this constitution,
can realize an apparatus capable of producing a pattern member at low cost with a
small number of processes.
[0022] The second production method of the methods of producing a pattern member of the
present invention for attaining the above-mentioned object comprises the steps of:
forming a plurality of single color transfer materials each having one of a plurality
of colors, by forming a coloring material layer of each color on each of a plurality
of transfer substrates;
forming a pattern by a process in which each surface of the single color transfer
materials of the plurality of colors is pressed by a pressing member having irregularity
of given pattern formed on its surface, to form an irregularity pattern corresponding
to the irregularity of the pressing member on the surface of the single color transfer
material; and
transferring a part of the coloring material layer to the transfer substrate to produce
a pattern member having a multi-color pattern of the plurality of colors on the substrate
by repeating, at frequency corresponding to the number of the plurality of colors
, an operation in which the surface of the single color transfer material of one color
among the single color transfer materials of a plurality of colors having an irregularity
pattern formed is overlapped on a given substrate and the coloring material layer
at the convex portion of the single color transfer material is transferred to the
substrate.
[0023] According to the second method of producing a pattern member of the present invention,
owing to the above-mentioned constitution, a pattern member having a fine pattern
can be produced at high productivity and low cost.
[0024] Here, the step of forming a plurality of single color transfer materials may be a
step in which a plastic deformation layer is formed on each of the above-mentioned
plurality of transfer substrates, and a coloring material layer of each color is formed
on the plastic deformation, to form a single color transfer material of a plurality
of colors.
[0025] When thus constituted, formation of an irregular pattern is easy due to the presence
of a plastic deformation layer, therefore, a pattern member can be produced at further
higher productivity and lower cost.
[0026] The step of forming a plurality of single color transfer materials may be a step
in which the above-mentioned plastic deformation layer and the above-mentioned coloring
material layer are overlapped and formed simultaneously.
[0027] When thus constituted, the number of processes can be decreased, therefore, a pattern
member can be produced at further higher productivity and lower cost.
[0028] The step of forming a plurality of single color transfer materials may be a step
in which a releasing layer is formed between the plastic deformation layer and coloring
material layer of each color.
[0029] When thus constituted, transfer of a coloring material layer to a substrate is easy,
therefore, a pattern member can be produced at further higher productivity and lower
cost.
[0030] Further, the step of forming a plurality of single color transfer materials may be
a step in which the plastic deformation layer, the releasing layer and the coloring
material layer are overlapped and formed simultaneously.
[0031] When thus constituted, a pattern member can be produced at further higher productivity
and lower cost.
[0032] The above-mentioned substrate is preferably a transparent substrate.
[0033] When thus constituted, a transparent pattern member can be produced at high productivity
and low cost.
[0034] Also, the substrate is preferably a substrate obtained by forming an electrode layer
on a transparent substrate.
[0035] When thus constituted, a pattern member having an electrode layer on its surface
can be produced at high productivity and low cost.
[0036] As described above, in the second method of producing a pattern member of the present
invention, only a coloring material layer may be formed on a substrate, a coloring
material layer and plastic deformation layer may be formed on a substrate, or a coloring
material layer, releasing layer and plastic deformation layer may be formed on a substrate,
further, a coloring material layer and releasing layer may be formed on a substrate.
[0037] Further, the first pattern member of the pattern members of the present invention
is a pattern member having a multi-color pattern made of color inks of a plurality
of colors on a substrate, formed by repeating, at frequency corresponding to the number
of the plurality of colors, an operation of overlapping a single color film of one
color among single color films of a plurality of colors having a color ink layer formed
on its surface by applying color inks of respective colors on a plurality of films
and drying the color inks, on a given substrate such that the color ink layer of the
single color film comes in contact with the substrate, and then, pressing the overlapped
substrate and the single color film by a pressing member having a convex portion of
given pattern formed on its surface, to transfer a portion corresponding to the pattern
of the convex portion of the color ink layer to the substrate.
[0038] Still further, the second pattern member of the pattern members of the present invention
is a pattern member having a multi-color pattern composed of a plurality of colors
on a substrate, formed by repeating, at frequency corresponding to the number of the
plurality of colors, an operation of pressing a surface of each single color transfer
material having one of the plurality of colors formed by forming a coloring material
layer of each color on each of a plurality of transfer materials, by a pressing member
having irregularity of given pattern formed on its surface, to form an irregularity
pattern corresponding to the irregularity of the pressing member on the surface of
the single color transfer material, and then, overlapping the surface of the single
color transfer material of one color among the single color transfer materials of
the plurality of colors having an irregularity pattern formed on a given substrate,
to transfer the coloring material layer at the convex portion of the single color
transfer material to the substrate.
[0039] According to the first and second pattern members owing to the above-mentioned constitution,
a pattern member can be obtained, at high productivity and low cost.
BRIEF DESCRIPTION OF THE DRAWINGS
[0040]
Figs. 1 to 4 are process views showing one embodiment of the method of producing a
multi-color pattern sheet of the present invention.
Fig. 5 is a view showing a pattern in the form of stripe of a multi-color pattern
sheet according to the present embodiment.
Fig. 6 is a view showing a pattern in the form of matrix of a multi-color pattern
sheet of the present embodiment.
Figs. 7 to 10 are schematic views according to various application modes adopted in
the present embodiment.
Fig. 11 is a schematic constitutional view showing one embodiment of the multi-color
pattern sheet production apparatus of the present invention.
Fig. 12 is a sectional view along the rotation axis direction of a patterning roll
in the present embodiment.
Fig. 13 is a part of a schematic process view showing the first embodiment of the
second method of producing a pattern member of the present invention.
Fig. 14 is a part of a schematic process view showing the first embodiment of the
second method of producing a pattern member of the present invention.
Fig. 15 is a part of a schematic process view showing the first embodiment of the
second method of producing a pattern member of the present invention.
Fig. 16 is a part of a schematic process view showing the first embodiment of the
second method of producing a pattern member of the present invention.
Fig. 17 is a part of a schematic process view showing the first embodiment of the
second method of producing a pattern member of the present invention.
Fig. 18 is a part of a schematic process view showing the first embodiment of the
second method of producing a pattern member of the present invention.
Fig. 19 is a part of a schematic process view showing the first embodiment of the
second method of producing a pattern member of the present invention.
Fig. 20 is a part of a schematic process view showing the second embodiment of the
second method of producing a pattern member of the present invention.
Fig. 21 is a part of a schematic process view showing the second embodiment of the
second method of producing a pattern member of the present invention.
Fig. 22 is a part of a schematic process view showing the second embodiment of the
second method of producing a pattern member of the present invention.
Fig. 23 is a part of a schematic process view showing the second embodiment of the
second method of producing a pattern member of the present invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0041] Here, a method of producing an organic thin film element utilizing the pattern member
production method of the present invention will be described, then, an organic thin
film layer transfer material will be described, further, an organic thin film element
will be described.
[1] Method of producing organic thin film element
[0042] A method of producing an organic thin film element of the present embodiment comprises
a process in which a plurality of transfer materials formed by forming an organic
thin film layer on a temporary substrate are used and an organic thin film layer is
transferred onto a substrate according to a releasing transfer method, and a process
in which a substrate carrying at least one of an electrode, transparent conductive
layer and organic thin film layer formed is pasted on the organic thin film layer
provided by a releasing transfer method.
[0043] The releasing transfer method is a transfer method in which a transfer material is
heated and/or pressed to soften an organic thin film layer and adhered on a film forming
surface of a substrate, then, a temporary supporting body is released to leave only
the organic thin film layer on the film forming surface. The pasting method is a method
in which the interfaces of at least two surfaces are connected by close adhesion,
crimping, fusion and the like.
Specifically, this is a method in which an organic thin film layer transferred on
a film forming surface, and a substrate having at least one of an electrode, transparent
conductive layer and organic thin film layer formed, are overlapped, then, heated
and/or pressed to soften the organic thin film layer which is adhered to the substrate
having at least one of an electrode, transparent conductive layer and organic thin
film layer formed. In the transfer method and pasting method used in the present embodiment
, heating and pressing may be used singly or in combination.
[0044] As the heating means, known methods can generally be used, and for example, a laminator,
infrared heater, roller heater, laser, thermal head and the like can be used. When
transfer of large area is conducted, sheet heating means are preferable, and a laminator,
infrared heater, roller heater and the like are more preferable. The transfer temperature
is not particularly restricted, and can be changed depending on the material of an
organic thin film layer and on a heating member, and in general, the temperature is
preferably from 40 to 250°C, further preferably from 50 to 200°C, particularly from
60 to 180°C. The preferable temperature range for transfer relates to the heat resistance
of a heating member, transfer material and substrate, and when the heat resistance
increases, the range changes according to the increase.
[0045] Though the pressing means is not particularly restricted, when a substrate liable
to be broken by strain such as glass and the like is used, the pressing means that
performs pressing uniformly is preferred. For example, it is preferable to use couple
rollers one or both of which are made of rubber, and specifically, laminators (Fast
Laminator VA-400III (manufactured by Taisei Laminator K.K.) and the like), thermal
heads for heat transfer printing, and the like can be used.
[0046] In the present embodiment, it is also possible to conduct transfer and releasing
processes repeatedly to laminate a plurality of organic thin film layers on a substrate.
The plurality of organic thin film layers may have the same composition or different
compositions. In the case of the same composition, there is a merit that lack of a
layer due to poor transfer or poor releasing can be prevented. In the case of layers
of different compositions, there can be provided a design by which functions are separated
to improved light emitting efficiency, for example, transparent conductive layer/light
emitting organic thin film layer/electron transporting organic thin film layer/electron
injection layer/backface electrode, transparent conductive layer/hole injection layer/hole
transporting organic thin film layer/light emitting organic thin film layer/electron
transporting organic thin film layer/electron injection layer/backface electrode,
can be laminated on a film forming surface by the transfer method of the present embodiment.
Regarding the transfer temperature in this procedure, it is preferable that temperature
for heating a prior transfer material is higher than temperature for heating the next
transfer material such that a prior transfer layer is not reverse-transferred to the
next transfer layer.
[0047] It is preferable, if necessary, to conduct re-heating on an organic thin film layer
transferred to a substrate, or on an organic thin film layer transferred onto the
previously transferred organic thin film layer. By re-heating, an organic thin film
layer is adhered more closely to a substrate or previously transferred organic thin
film layer. It is preferable, if necessary, to conduct pressing in re-heating. The
re-heating temperature is preferably in the range of the transfer temperature ± 50°
C.
[0048] A surface treatment for improving close adhesive force may be performed on a film
forming surface between a prior transfer process and the next transfer process such
that a prior transfer layer is not reverse-transferred to the next transfer layer.
As such a surface treatment, for example, activation treatments such as a corona discharge
treatment, flame treatment, glow discharge treatment, plasma treatment and the like
are listed. When a surface treatment is used together, it may be permissible that
the transfer temperature of a prior transfer material is lower than the transfer temperature
of the next transfer material as long as no reverse-transfer occurs.
[0049] As the apparatus of producing an organic thin film element, an apparatus of feeding
a transfer material obtained by forming an organic thin film layer on a temporary
supporting body, an apparatus of pressing a transfer material while heating to the
film forming surface of a substrate to transfer an organic thin film layer to the
film forming surface of a substrate, and an apparatus of peeling the temporary supporting
body from the organic thin film layer after transfer, can be used.
[0050] The production apparatus used in the present embodiment preferable has means of pre-heating
a transfer material and/or substrate before feeding to a transfer apparatus. Further,
it is preferable that a cooling apparatus is contained in the latter stage of the
transfer apparatus.
[0051] It is preferable that an approach angle controlling portion for controlling the approach
angle to a substrate of a transfer material to 90° or less, is provided in front of
a transfer apparatus. Further, it is preferable that a releasing angle controlling
portion for controlling the releasing angle to an organic thin film layer of a temporary
supporting body to 90° or more, is provided at the rear surface of a transfer apparatus
or cooling apparatus. Details of these organic thin film element production methods
and apparatuses are described in JP-A No. 2001-089663, and the like.
[2] Transfer material
(1) Constitution
[0052] As the transfer material, that having an organic thin film layer on a temporary supporting
body is used. The transfer material can be produced appropriately using a known method,
and it is preferable to use a wet method from the standpoint of productivity. Transfer
materials having an organic thin film layer provided may be produced individually
as an independent transfer material or may be produced in the surface order. Namely,
it may also be permissible that a plurality of organic thin film layers are provided
on one temporary supporting body. If this transfer material is used, a plurality of
organic thin film layers can be formed continuously without requiring exchange of
the transfer material.
[0053] Further, if a transfer material obtained by previously laminating two or more organic
thin film layers on a temporary supporting body is used, a multi-layer film can be
laminated on the film forming surface of a substrate in one transfer process. When
previous lamination is conducted on a temporary supporting body, if the interface
of each organic thin film layer laminated is not uniform, movement of holes and electrons
becomes irregular. Therefore, it is necessary to deliberately select a solvent for
uniformalizing the interface and it is necessary to select an organic compound for
the organic thin film layer soluble in its solvent.
(2) Temporary supporting body
[0054] The temporary supporting body used in the present embodiment should be constituted
of a material stable chemically and thermally and having flexibility, and specifically
preferable are thin sheets made of fluorine resins [for example, ethylene tetrafluoride
resin (PTFE), ethylene trifluoride chloride resin (PCTFE)], polyesters (for example,
polyethylene terephthalate, polyethylene naphthalate (PEN)), polyarylates, polycarbonates,
polyolefins (for example, polyethylene, polypropylene), polyether sulfone (PES) and
the like, and laminates of them. The thickness of a temporary supporting body is suitably
from 1 µm to 100 µm, further preferably from 2 µm to 50 µm, particularly preferably
from 3 µm to 30 µm.
(3) Formation of organic thin film layer on temporary supporting body
[0055] An organic thin film layer containing a polymer compound as a binder is preferably
formed on a temporary supporting body by a wet method. For this, a material for organic
thin film layer is dissolved in an organic solvent to give desired concentration,
and the resulted solution is applied on a temporary supporting body. The application
method is not particularly restricted as long as the dry film thickness of an organic
thin film layer is 200 nm or less and uniform film thickness distribution is obtained,
and includes a spin coat method, gravure coat method, die coat method, bar coat method
and the like.
(4) Organic thin film layer
[0056] The organic thin film layer is a layer constituting an organic thin film element,
and examples thereof include a light emitting organic thin film layer, electron transporting
organic thin film layer, hole transporting organic thin film layer, electron injection
layer, hole injection layer and the like from the standpoint of their properties.
The organic thin film layer does not have a light-heat conversion layer (layer capable
of performing light-heat conversion by laser). Further, there are various layers for
improving a color developing property. Specific examples of the compound used in each
layer are described in, for example, "Monthly Display", October 1998, separate volume
"Organic EL Display" (published by Techno Times Co.Ltd), and the like.
[0057] The glass transition temperature of an organic thin film layer itself or components
in this is preferably not lower than 40° C and not higher than the transition temperature
+40° C, further preferably not lower than 50° C and not higher than the transition
temperature +20° C, particularly preferably not lower than 60°C and not higher than
the transition temperature. The flow initiation temperature of an organic thin film
layer itself in a transition material or components in this is preferably not lower
than 40°C and not higher than the transition temperature +40°C, further preferably
not lower than 50°C and not higher than the transition temperature +20° C, particularly
preferably not lower than 60° C and not higher than the transition temperature. The
glass transition temperature can be measured by a differential scanning calorimeter
(DSC). The flow initiation temperature can be measured using Flow Testor CFT-500 manufactured
by Shimadzu Corporation.
(a) Light emitting organic thin film layer
[0058] As the light emitting organic thin film layer, that containing at least one kind
of light emitting compound is used. The light emitting compound is not particularly
restricted, may be a fluorescence emitting compound or a phosphorescence emitting
compound. Alternatively, a fluorescence emitting compound and a phosphorescence emitting
compound may be used simultaneously. In the present embodiment, it is preferable to
use a phosphorescence emitting compound from the standpoints of light emitting brilliance
and light emitting efficiency.
[0059] As the phosphorescence emitting compound, benzooxazole derivatives, benzimidazole
derivatives, benzothiazole derivatives, styrylbenzene derivatives, polyphenyl derivatives,
diphenylbutadiene derivatives, tetraphenylbutadiene derivatives, naphthalimide derivatives,
coumarin derivative, perylene derivatives, perynone derivatives, oxadiazole derivatives,
aldazine derivatives, pyralidine derivatives, cyclopentadiene derivatives, bisstyrylanthracene
derivatives, quinacridone derivatives, pyrrolopyridine derivatives, thiadiazolopyridine
derivatives, styrylamine derivatives, aromatic dimethylidene compounds, metal complexes
(metal complexes of 8-quinolinol derivatives, rare earth metal complexes, and the
like), polymer light emitting compounds (polythiophene derivatives, polyphenylene
derivatives, polyphenylenevinylene derivatives, polyfluorene derivatives and the like)
and other compounds can be used. These may be used singly or in admixture of two or
more.
[0060] The phosphorescence emitting compound is preferably a compound capable of emitting
light from the triplet excited state, and preferable are orthometalated complexes
and porphyrin complexes. Of porphyrin complexes, a porphyrin platinum complex is preferable.
The phosphorescence emitting compounds may be used alone or in combination of two
or more.
[0061] The orthometalated complex referred to in the present embodiment is a generic name
for the group of compounds described in Akio Yamamoto, "Organic Metal Chemistry, Base
and Application (Yuki Kinzoku Kagaku, Kiso to Oyo)", pp. 150 and 232, published by
Shokabo (1982), H. Yersin, "Photochemistry and Photophysics of Coordination Compounds",
pp. 71 to 77 and 135 to 146, Springer-Verlag (1987) and the like. The ligand forming
the orthometalated complex is not particularly restricted, and preferably a 2-phenylpyridine
derivative, 7,8-benzoquinoline derivative, 2-(2-thienyl)pyridine derivative, 2-(1-naphthyl)pyridine
derivative or 2-phenylquinoline derivative. These derivatives may have a substituent.
In addition to ligands essential for forming these orthometalated complexes, other
ligands may be present. As the center metal forming the orthometalated complex, any
transition metal can be used, and in the present embodiment, rhodium, platinum, gold,
iridium, ruthenium, palladium and the like can be preferably used. An organic thin
film layer containing such an orthometalated complexis excellent in light emitting
brilliance and light emitting efficiency. The orthometalated complex is described
specifically in Japanese Patent Application No. 2000-254171.
[0062] The orthometalated complex used in the present embodiment can be synthesized by known
methods described in Inorg. Chem., 30, 1685, 1991, Inorg. Chem., 27, 3464, 1988, Inorg.
Chem., 33, 545, 1994, Inorg. Chim. Acta, 181, 245, 1991, J. Organomet. Chem., 335,
293, 1987, J. Am. Chem. Soc., 107, 1431, 1985 and the like.
[0063] The content of a light emitting compound in a light emitting organic thin film layer
is not particularly restricted, and for example, preferably from 0.1 to 70 wt%, more
preferably from 1 to 20 wt%. When the content of a light emitting compound is less
than 0.1 wt% or over 70 wt%, its effect may not be sufficiently manifested.
[0064] The light emitting organic thin film layer may contain host compounds, hole transporting
materials, electron transporting materials, electrically inactive polymer binders
and the like, if necessary. Functions of these materials can be attained simultaneously
by one compound in some cases. For example, a carbazole derivative functions not only
as a host compound but also as a hole transporting compound.
[0065] The host compound is a compound causing energy movement from its excited state to
a light emitting compound, resultantly to cause light emission of this light emitting
compound. Specific examples thereof include carbazole derivatives, triazole derivatives,
oxazole derivatives, oxadiazole derivatives, imidazole derivatives, polyarylalkane
derivatives, pyrazoline derivatives, pyrazolone derivatives, phenylenediamine derivatives,
arylamine derivatives, amino-substituted chalcone derivatives, styrylanthracene derivatives,
fluorenone derivatives, hydrazone derivatives, stilbene derivatives, silazane derivatives,
aromatic tertiary amine compounds, styrylamine compounds, aromatic dimethylidene compounds,
porphyrin compounds, anthraquinodimethane derivatives, anthrone derivatives, diphenylquinone
derivatives, thiopyranedioxide derivatives, carbodiimide derivatives, fluorenylidenemethane
derivatives, distyrylpyrazine derivatives, heterocyclic tetracarboxylic anhydrides
such as naphthaleneperylene and the like, phthalocyanine derivatives, metal complexes
of 8-quinolinol derivatives, metal complexes having as a ligand metalphthalocyanine,
benzooxazole, benzothiazole and the like, polysilane compounds, poly(N-vinylcarbazole)
derivatives, conductive polymers such as aniline copolymers, thiophene oligomers,
polythiophene and the like, polythiophene derivatives, polyphenylene derivatives,
polyphenylenevinylene derivatives, polyfluorene derivatives and the like. The host
compound may be used alone or in combination of two or more. The content of the host
compound in a light emitting organic thin film layer is preferably from 0 to 99.9
wt%, more preferably from 0 to 99.0 wt%.
[0066] The hole transporting material is not particularly restricted as long as it has any
of a function of injecting a hole from an anode, a function of transporting a hole
and a function of blocking an electron injected from a cathode, and may be a low molecular
weight material or high molecular weight material. Specific examples thereof include
carbazole derivatives, triazole derivatives, oxazole derivatives, oxadiazole derivatives,
imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives, pyrazolone
derivatives, phenylenediamine derivatives, arylamine derivatives, amino-substituted
chalcone derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone
derivatives, stilbene derivatives, silazane derivatives, aromatic tertiary amine compounds,
styrylamine compounds, aromatic dimethylidene compounds, porphyrin compounds, polysilane
compounds, poly(N-vinylcarbazole) derivatives, conductive polymers such as aniline
copolymers, thiophene oligomers, polythiophene and the like, polythiophene derivatives,
polyphenylene derivatives, polyphenylenevinylene derivatives, polyfluorene derivatives
and the like. These may be used alone or in combination of two or more. The content
of the hole transporting material in a light emitting organic thin film layer is preferably
from 0 to 99.9 wt%, more preferably from 0 to 80.0 wt%.
[0067] The electron transporting material is not particularly restricted as long as it has
any of a function of injecting an electron from a cathode, a function of transporting
an electron and a function of blocking a hole injected from an anode. Specific examples
thereof include triazole derivatives, oxazole derivatives, oxadiazole derivatives,
fluorenone derivatives, anthraquinodimethane derivatives, anthrone derivatives, diphenylquinone
derivatives, thiopyranedioxide derivatives, carbodiimide derivatives, fluorenylidenemethane
derivatives, distyrylpyrazine derivatives, heterocyclic tetracarboxylic anhydrides
such as naphthaleneperylene and the like, phthalocyanine derivatives, metal complexes
of 8-quinolinol derivatives, metal complexes having as a ligand metalphthalocyanine,
benzooxazole, benzothiazole and the like, conductive polymers such as aniline copolymers,
thiophene oligomers, polythiophene and the like, polythiophene derivatives, polyphenylene
derivatives, polyphenylenevinylene derivatives, polyfluorene derivatives and the like.
These may be used alone or in combination of two or more. The content of the electron
transporting material in a light emitting organic thin film layer is preferably from
0 to 99.9 wt%, more preferably from 0 to 80.0 wt%.
[0068] As the polymer binder, polyvinyl chloride, polycarbonate, polystyrene, polymethyl
methacrylate, polybutyl methacrylate, polyester, polysulfone, polyphenylene oxide,
polybutadiene, hydrocarbon resin, ketone resin, phenoxy resin, polyamide, ethylcellulose,
vinyl acetate, ABS resin, polyurethane, melamine resin, unsaturated polyester, alkyd
resin, epoxy resin, silicone resin, polyvinylbutyral, polyvinylacetal and the like
can be used. These may be used alone or in combination of two or more. A light emitting
organic thin film layer containing a polymer binder can be easily formed by application
in large area by a wet film forming method.
[0069] The thickness of a light emitting organic thin film layer is preferably from 10 nm
to 200 nm, more preferably from 20 nm to 80 nm. When the thickness is over 200 nm,
driving voltage may increase. On the other hand, when less than 10 nm, an organic
thin film element may form a short circuit.
(b) Hole transporting organic thin film layer
[0070] The organic thin film layer may have a hole transporting organic thin film layer
composed of the above-mentioned hole transporting material, if necessary. The hole
transporting organic thin film layer may contain the above-mentioned polymer binder.
The thickness of the hole transporting organic thin film layer is preferably from
10 nm to 200 nm, more preferably from 20 nm to 80 nm. When the thickness is over 200
nm, driving voltage may increase, and when less than 10 nm, an organic thin film element
may give a short circuit.
(c) Electron transporting organic thin film layer
[0071] The organic thin film element may have an electron transporting organic thin film
layer composed of the above-mentioned electron transporting material, if necessary.
The electron transporting organic thin film layer may contain the above-mentioned
polymer binder. The thickness of the electron transporting organic thin film layer
is preferably from 10 nm to 200 nm, more preferably from 20 nm to 80 nm. When the
thickness is over 200 nm, driving voltage may increase, and when less than 10 nm,
an organic thin film element may give a short circuit.
[0072] When an organic thin film layer is formed by application by a wet film forming method,
a solvent used to dissolve a material of an organic thin film layer to prepare an
application solution is not particularly restricted, and can be appropriately selected
depending on the kind of the hole transporting material, orthometalated complex, host
compound, polymer binder and the like. Exemplified are halogen-based solvents (chloroform,
carbon tetrachloride, dichloromethane, 1,2-dichloroethane, chlorobenzene and the like),
ketone-based solvents (acetone, methyl ethyl ketone, diethylketone, n-propyl methyl
ketone, cyclohexanone and the like), aromatic solvents (benzene, toluene, xylene and
the like), ester-based solvents (ethyl acetate, n-propyl acetate, n-butyl acetate,
methyl propionate, ethyl propipnate, γ-butyrolactone, diethyl carbonate and the like),
ether-based solvents (tetrahydrofuran, dioxane, and the like), amide-based solvents
(dimethylformamide, dimethylacetamide and the like), dimethyl sulfoxide, water and
the like. The solid content in an application solution for organic thin film layer
is not particularly restricted, and its viscosity can also be optionally selected
depending on a wet film forming method.
[0073] When a plurality of organic thin film layers are formed, dry film forming methods
such as a vapor deposition method, sputter method and the like, wet film forming methods
such as dipping, spin coat method, dip coat method, cast method, die coat method,
roll coat method, bar coat method, gravure coat method and the like, printing methods,
and the like can also be used together, in addition to a transfer method.
[3] Organic thin film element
(1) Constitution
[0074] The whole constitution of the organic thin film element may be a constitution in
which transparent conductive layer/light emitting organic thin film layer/backface
electrode, transparent conductive layer/light emitting organic thin film layer/electron
transporting organic thin film layer/backface electrode, transparent conductive layer/hole
transporting organic thin film layer/light emitting organic thin film layer/electron
transporting organic thin film layer/backface electrode, transparent conductive layer/hole
transporting organic thin film layer/light emitting organic thin film layer/backface
electrode, transparent conductive layer/light emitting organic thin film layer/electron
transporting organic thin film layer/electron injection layer/backface electrode,
transparent conductive layer/hole injection layer/hole transporting organic thin film
layer/light emitting organic thin film layer/electron transporting organic thin film
layer/electron injection layer/backface electrode, and the like are laminated in this
order on a substrate supporting body, a constitution of reverse lamination of them,
and the like. The light emitting organic thin film layer contains a fluorescence emitting
compound and/or phosphorescence emitting compound, and usually, light emission is
derived from a transparent conductive layer. Specific examples of the compound used
in each layer are described in, for example, "Monthly Display", October 1998, separate
volume "Organic EL Display" (published by Techno Times Co. Ltd), and the like.
(2) Substrate supporting body
[0075] The substrate supporting body may be made of an inorganic material such as yttrium
stabilized with zirconia (YSZ), glass and the like, polyester such as polyethylene
terephthalate, polybutylene terephthalate, polyethylene naphthalate and the like,
polymer material such as polystyrene, polycarbonate, polyether sulfone, polyarylate,
allyl diglycol carbonate, polyimide, polycycloolefin, norbornene resin, polychlorotrifluoroethylene,
Teflon (trade mark), polytetrafluoroethylene-polyethylene copolymer and the like,
metal foil such as aluminum foil, copper foil, stainless foil, gold foil, silver foil
and the like, polyimide, plastic sheet of liquid crystal polymer, and the like. In
the present embodiment, it is preferable to use a flexible substrate supporting body
since it is not easily broken, is easily bended, and is light, and the like. Preferable
as the material forming such a substrate supporting body are polyimides, polyesters,
polycarbonates, polyether sulfone, metal foils (aluminum foil, copper foil, stainless
foil, gold foil, silver foil and the like), plastic sheets of liquid crystalline polymers,
polymer materials containing a fluorine atom (polychlorotrifluoroethylene, Teflon
(trade mark), polytetrafluoroethylene-polyethylene copolymer, and the like) and other
compounds, excellent in heat resistance, dimension stability, solvent resistance,
electric insulation property and processability and having low gas permeability and
low hygroscopicity.
[0076] The form, structure, size and the like of the substrate supporting body can be appropriately
selected depending on the object and application of an organic thin film element.
The form is plate in general. The structure may be a single layer structure or a laminated
structure. The substrate supporting body may be formed of a single member or of two
or more members. As the substrate supporting body, any of a transparent body and a
non-transparent body can be used. However, when light emission is derived from the
supporting body side since a transparent electrode described below is situated at
the substrate supporting body side against an organic layer containing a light emitting
layer, and the like, it is preferable that the substrate supporting body is colorless
and transparent or colored and transparent, and from the standpoint of suppression
of scattering and attenuation of light, colorless and transparent is preferable.
[0077] As the flexible substrate supporting body which does not give a short circuit in
forming an electrode to produce a light emitting element, a substrate supporting body
provided with an insulation layer on one or both surfaces of a metal foil is preferable.
The metal foil is not particularly restricted, and a metal foil such as an aluminum
foil, copper foil, stainless foil, gold foil, silver foil and the like can be used.
Of them, from the standpoints of easiness in processing and cost, an aluminum foil
or a copper foil is preferable. The insulation layer is not particularly restricted,
and can be formed of, for example, an inorganic substance such as inorganic oxides,
inorganic nitrides and the like, a polyester such as polyethylene terephthalate, polybutylene
phthalate, polyethylene naphthalate and the like, a plastic such as polystyrene, polycarbonate,
polyether sulfone, polyarylate, allyl diglycol carbonate, polyimide, polycycloolefin,
norbornene resin, poly(chlorotrifluoroethylene), polyimide and the like.
[0078] The substrate supporting body has a coefficient of linear expansion by heat, preferably
20 ppm/°C or less. The coefficient of linear expansion by heat is measured by a method
in which a sample is heated at constant speed and change in length of the sample is
detected, and mainly, it is measured by TMA method. When the coefficient of linear
expansion by heat is over 20 ppm/°C, becomes a cause for peeling of an electrode and
organic thin film layer due to heat and the like in a pasting process or in use, and
the like and becomes a cause for deterioration in durability.
[0079] The coefficient of linear expansion by heat of an insulation layer provided on a
substrate supporting body is also preferably 20 ppm/°C or less. As the material forming
an insulation layer having a coefficient of linear expansion by heat of 20 ppm/°C
or less, metal oxides such as silicon oxide, germanium oxide, zinc oxide, aluminum
oxide, titanium oxide, copper oxide and the like, and metal nitrides such as silicon
nitride, germanium nitride, aluminum nitride and the like, are preferable, and these
can be used alone or in combination of two or more. The thickness of the inorganic
insulation layer made of a metal oxide and/or metal nitride is preferably from 10
nm to 1000 nm. When the inorganic insulation layer is thinner than 10 nm, an insulation
property is too low. When the inorganic insulation layer is thicker than 1000 nm,
crack tends to occur, and pin holes are formed to decrease an insulation property.
The method of forming the insulation layer made of a metal oxide and/or metal nitride
is not particularly restricted, and dry methods such as a vapor deposition method,
sputtering method, CVD method and the like, wet methods such as a sol-gel method and
the like, a method in which particles of a metal oxide and/or metal nitride are dispersed
in a solvent and the resulted solution is applied, and the like can be used.
[0080] As the plastic material having a coefficient of linear expansion by heat of 20 ppm
or less, particularly, a polyimide and a liquid crystal polymer can be preferably
used. Details such as properties and the like of these plastic materials are described
in "Plastic Data Book" (Asahi Kasei Amidas Corporation., "Plastic" editorial division,
edit), and the like. When a polyimide and the like are used as an insulation layer,
it is preferable that a sheet made of a polyimide and the like and an aluminum foil
are laminated. The thickness of a sheet made of a polyimide is preferably from 10
µm to 200 µm. When the thickness of a sheet made of a polyimide is smaller than 10
µm, handling in lamination becomes difficult. When the thickness of a sheet made of
a polyimide and the like is larger than 200 µm, flexibility disappears, and handling
becomes inconvenient. The insulation layer may be provided only on one surface of
a metal foil, or may be provided on both surfaces of a metal foil. When provided on
both surfaces, the both surfaces may be made of a metal oxide and/or metal nitride,
or, the both surfaces may be a plastic insulation layer such as a polyimide insulation
layer. Further, it may also be permissible that one surface is an insulation layer
made of a metal oxide and/or metal nitride, and other surface is a polyimide sheet
insulation layer. If necessary, a hard coat layer and under coat layer may also be
provided.
[0081] A wet permeation preventing layer (gas barrier layer) may also be provided on the
electrode side surface, surface opposite to an electrode, or both of them. As the
material constituting the wet permeation preventing layer, inorganic substances such
as silicon nitride, silicon oxide and the like are preferably used. The wet permeation
preventing layer can be formed by a high frequency sputtering method and the like.
On the substrate supporting body, a hard coat layer and under coat layer may also
be provided, if necessary.
[0082] Furthermore, a substrate provided with an insulation layer on one or both of surfaces
of a metal foil is preferable. The metal foil is not particularly restricted, and
metal foils such as an aluminum foil, copper coil, stainless foil, gold foil, silver
foil and the like can be used. Among others, from the standpoints of easiness in processing
and cost, an aluminum foil or copper foil is preferable. The insulation layer is not
particularly restricted, and can be formed of, for example, an inorganic substance
such as inorganic oxides, inorganic nitrides and the like, a polyester such as polyethylene
terephthalate, polybutylene phthalate, polyethylene naphthalate and the like, a plastic
such as polystyrene, polycarbonate, polyether sulfone, polyarylate, allyl diglycol
carbonate, polyimide, polycycloolefin, norbornene resin, poly(chlorotrifluoroethylene),
polyimide and the like.
[0083] The moisture permeability of the substrate supporting body is preferably 0.1 g/m
2·day or less, and more preferably 0.05 g/m
2·day or less, particularly preferably 0.01 g/m
2·day or less. The oxygen permeability is preferably 0.1 ml/m
2·day/atm or less, more preferably 0.05 ml/m
2·day/atm or less, particularly preferably 0.01 ml/m
2·day/atm or less. The moisture permeability can be measured by a method according
to JIS K7129B method (mainly, MOCON method). The oxygen permeability can be measured
by a method according to JIS K7126B method (mainly, MOCON method). By such limitation,
invasion of moisture and oxygen into a light emitting element, causing deterioration
of durability can be prevented.
(3) Electrode (cathode or anode)
[0084] Any of a transparent conductive layer and backface electrode can be used as a cathode
or an anode, and this selection is determined depending on the composition constituting
an organic thin film element. Usually, the anode may only have a function as a cathode
of supplying a hole to an organic thin film layer, and its form, structure, size and
the like are not particularly restricted, and the anode can be appropriately selected
from known electrodes depending on the object and application of a light emitting
element.
[0085] As the material forming the cathode, metal single bodies, alloys, metal oxides, electric
conductive compounds, mixtures thereof, and the like can be used, and preferably,
materials having a work function of 4.5 eV or less are used. Specific examples thereof
include alkali metals (for example, Li, Na, K. Cs and the like), alkaline earth metals
(for example, Mg, Ca and the like), gold, silver, lead, aluminum, sodium-potassium
alloy, lithium-aluminum alloy, magnesium-silver alloy, indium, rare earth metals (ytterbium
and the like), and the like. These may be used singly, and from the standpoint of
simultaneous satisfaction of stability and electron injectability, it is preferable
to use two or more of them in combination.
[0086] Of them, alkali metals and alkaline earth metals are preferable from the standpoint
of electron injectability, and materials mainly composed of aluminum are preferable
from the standpoint of storage stability. Herein, the materials mainly composed of
aluminum include not only aluminum alone, but also alloys of aluminum with an alkali
metal or alkaline earth metal in an amount of 0.01 wt% to 10 wt% (for example, lithium-aluminum
alloy, magnesium-aluminum alloy and the like) or mixtures thereof.
[0087] When light is derived from the cathode side, it is necessary to use a transparent
cathode. The transparent cathode may advantageously be substantially transparent to
light. For simultaneous satisfaction of electron injectability and transparency, a
two-layer structure composed of a thin film metal layer and a transparent conductive
layer can also be used. The material of the thin film metal layer is described in
detail in JP-A Nos. 2-15595 and 5-121172. The thickness of the above-mentioned thin
film metal layer is preferably from 1 nm to 50 nm. When less than 1 nm, it is difficult
to produce a thin film layer uniformly. When thicker than 50 nm, transparency to light
deteriorates.
[0088] The material used in the transparent conductive layer is not particularly restricted
as long as it is a transparent material having conductivity or semi-conductivity,
and the above-mentioned materials used in an anode can be preferably used. Listed
as the preferable material are tin oxide doped with antimony, fluorine and the like
(ATO, FTO, etc.), tin oxide, zinc oxide, indium oxide, indium tin oxide (ITO), indium
zinc oxide (IZO), and the like. The thickness of the transparent conductive layer
is preferably from 30 nm to 500 nm. When the thickness of the transparent conductive
layer is smaller than 30 nm, conductivity or semi-conductivity is poor, and when larger
than 500 nm, productivity is poor.
[0089] The method of forming a cathode is not particularly restricted, and known methods
can be adopted, and it is preferable to conduct the formation in a vacuum apparatus.
For example, this formation method is appropriately selected from physical methods
such as a vacuum vapor deposition method, sputtering method, ion plating method and
the like and chemical methods such as CVD, plasma CVD and the like, in view of compatibility
with the material in cathode. For example, when metals and the like are selected as
the material of a cathode, one or more kinds of metals can be treated simultaneously
or sequentially by sputtering and the like. When an organic conductive material is
used, a wet film formation method may also be used.
[0090] Patterning of a cathode can be conducted by chemical etching by photolithography
and the like, physical etching using laser and the like, a vacuum vapor deposition
method using a mask, a sputtering method, or a liftoff method, a printing method and
the like.
[0091] A dielectric layer having a thickness of 0.1 nm to 5 nm made of a fluoride of an
alkali metal or alkaline earth metal may be inserted between a cathode and an organic
thin film layer. The dielectric layer can be formed, for example, by a vacuum vapor
deposition method, sputtering method, ion plating method and the like.
(4) Patterning
[0092] In this case, a multi-color patterning method of the present embodiment is applied.
Namely, a pattern corresponding to a plurality of colors is formed by the following
processes. Details thereof are shown in examples described later.
i) On a temporary supporting body, three kinds of single color films applied at uniform
film thickness are produced corresponding to RGB.
ii) An applied surface of one kind of single color film is overlapped on a sheet to
be subjected to patterning.
iii) Pressing is effected by a pressing member having a convex portion of given pattern
formed from the rear side of a single color film, to transfer only pattern parts corresponding
to the convex portion to a sheet.
iv) Further, for another single color film, pattern parts are transferred to a sheet
in the same manner as in the process iii).
Here, in this procedure, the position of the pattern transferred in the process iii)
is read and given positioning is conducted before the transfer.
v) Transfer for a third color is conducted in the same manner as in the process iv).
[0093] By this, a patterned organic thin film layer carrying a plurality of organic thin
film layers formed having different compositions can be produced.
(5) Other layers
[0094] As the layer constituting an organic thin film element, a protective layer and a
sealing layer are preferably provided for preventing deterioration in a light emitting
ability. Further, in a transfer material, a releasing layer may be provided between
a temporary supporting body and an organic thin film layer and an adhesive layer may
be provided between an organic thin film layer and a film forming surface for improving
transferability as long as a light emitting ability is not affected.
(a) Protective layer
[0095] The organic thin film element may have a protective layer described in JP-A Nos.
7-85974, 7-192866, 8-22891, 10-275682, 10-106746 and the like. The protective layer
is formed on the uppermost surface of an organic thin film element. Here, the uppermost
surface indicates the outer side surface of a backface electrode when a substrate
supporting body, transparent conductive layer, organic thin film layer and backface
electrode are laminated in this order, for example, and indicates the outer side surface
of a transparent conductive layer when a substrate supporting body, backface electrode,
organic thin film layer and transparent conductive layer are laminated in this order.
The form, size, thickness and the like of the protective layer are not particularly
restricted, The material constituting the protective layer is not particularly restricted
as long as it has a function to suppress invasion or permeation of substances deteriorating
an organic thin film element such as moisture, oxygen and the like into an element,
and for example, silicon monoxide, silicon dioxide, germanium monoxide, germanium
dioxide and the like can be used.
[0096] The method of forming the protective layer is not particularly restricted, and for
example, a vacuum vapor deposition method, sputtering method, reactive sputtering
method, molecule beam epitaxy method, cluster ion beam method, ion plating method,
plasma polymerization method, plasma CVD method, laser CVD method, thermal CVD method,
coating method and the like can be applied.
(b) Sealing layer
[0097] It is preferable to provide a sealing layer for preventing invasion of moisture and
oxygen, on an organic thin film element. As the material forming the sealing layer,
copolymers of tetrafluoroethylene and at least one comonomer, fluorine-containing
copolymers having a cyclic structure in the copolymerization main chain, copolymers
of polyethylene, polypropylene, polymethyl methacrylate, polyimide, polyurea, polytetrafluoroethylene,
polychlorotrifluoroethylene, polydichlorodifluoroethylene, chlorotrifluoroethylene
or dichlorodifluoroethylene with other comonomers, water-absorbing substances having
a water absorption coefficient of 1% or more, moisture proof substances having a water
absorption coefficient of 1% or less, metals (In, Sn, Pb, Au, Cu, Ag, Al, Ti, Ni and
the like), metal oxides (MgO, SiO, SiO
2, Al
2O
3, GeO, NiO, CaO, BaO, Fe
2O
3, Y
2O
3, TiO
2 and the like), metal fluorides (MgF
2, LiF, AlF
3, CaF
2 and the like), liquid carbon fluorides (perfluoroalkanes, perfluoroamines, perfluoro
ethers and the like), those obtained by dispersing an absorbing agent for moisture
and oxygen in a liquid carbon fluoride, and the like can be used.
[0098] For the purpose of blocking moisture and oxygen from outside, an organic thin film
layer is preferably sealed with a sealing members such as a sealing plate, sealing
vessel and the like. A sealing member may be provided only at the backface electrode
side, or the whole light emitting laminate may be coated with a sealing member. The
form, size, thickness and the like of the sealing member are not particularly restricted
as long as it can seal an organic thin film layer and can block air from outside.
As the material used in the sealing member, glass, stainless steel, metals (aluminum,
and the like), plastics (polychlorotrifluoroethylene, polyesters, polycarbonates,
and the like), ceramics and the like can be used.
[0099] In providing a sealing member on a light emitting laminate, a sealing agent (adhesive)
may be appropriately used. When the whole light emitting laminate is coated with a
sealing member, sealing members may be mutually thermally fused without using a sealing
agent. As the sealing agent, an ultraviolet-hardening resin, thremosetting resin,
two pack type hardening resin and the like can be used.
[0100] Further, a moisture absorbent or inert liquid may be inserted in a space between
a sealing container and an organic thin film element. The moisture absorbent is not
particularly restricted, and specific examples thereof include barium oxide, sodium
oxide, potassium oxide, calcium oxide, sodium sulfate, calcium sulfate, magnesium
sulfate, phosphorus pentoxide, calcium chloride, magnesium chloride, copper chloride,
cesium fluoride, niobium fluoride, calcium bromide, vanadium bromide, molecular sieve,
zeolite, magnesium oxide and the like. As the inert liquid, paraffins, liquid paraffins,
fluorine-based solvents (perfluoroalkanes, perfluoroamines, perfluoro ethers and the
like), chlorine-based solvents, silicone oils and the like can be used.
[0101] The light emitting element in the present embodiment can be allowed to emit light
by applying direct voltage (alternating current component may be contained, if necessary)
(usually from 2 V to 4 V) or direct current between a cathode and an anode. For driving
the light emitting element, methods described in JP-A Nos. 2-148687, 6-301355, 5-29080,
7-134558, 8-234685 and 8-241047, US Patent Nos. 5828429 and 6023308, Japanese Patent
No. 2784615, and the like can be utilized.
EXAMPLES
[0102] Regarding embodiments of the present invention, only contents described in the above-mentioned
"patterning" column will be described below.
[0103] Figs 1 to 4 are process views showing a method of producing a multi-color pattern
member which is one embodiment of the method of producing a pattern member of the
present invention.
[0104] Fig. 1 shows three kinds of single color films 11a, 11b and 11c produced by a single
color film production process. In the single color film production process of the
present embodiment, three inks of RGB (light emitting materials) are applied on a
film 10, and dried, to produce three kinds of single color films 11a, 11b and 11c
carrying RGB three color ink layers 12a, 12b and 12c respectively formed on the surface.
These are sheets called temporary supporting body in the above-mentioned description.
Details of the method of applying them will be described later.
[0105] Then, the transfer process will be explained.
[0106] Figs. 2 to 3 show a transfer process. In this transfer process, a single color film
of one color among the above-mentioned three kinds of single color films 11a, 11b
and 11c, for example, a single color film 11a of R color, is overlapped on a sheet
20 such that a color ink layer 12a of the single color film 11a comes in contact with
the sheet 20, and the overlapped sheet 20 and single color film 11a are pressed by
a pressing member 30 having a convex portion 23 of given pattern formed on its surface,
from the rear surface 13a against the surface on which the color ink layer 12a of
the single color film 11a is formed, to transfer parts corresponding to the pattern
of the convex portion 23 of the color ink layer 12a to the sheet 20, and this operation
is repeated for RGB three colors, to produce a multi-color pattern sheet 21 carrying
patterns 21a, 21b and 21c made of three color ink layers of RGB of given pattern formed
on the sheet 20, as shown in Fig. 4. This multi-color pattern sheet 21 is one example
of the pattern member referred in the present invention.
[0107] The sheet 20 is one example of the substrate referred in the present invention, and
as the sheet 20, materials such as resins, metals, glass and the like can be used.
[0108] As the transfer mode, a transfer mode using pressing means and heating means together
is preferable.
[0109] As the pressing member 30, a multi-color pattern sheet can also be produced according
to batch mode by using a flat plate and the like, however, it is preferable to produce
a multi-color pattern sheet by using, as the pressing member 30, transfer means composed
of a patterning roll having a convex portion of given pattern formed on its surface
and a counter roll as in a multi-color pattern sheet production apparatus shown in
Fig. 11, as a continuous process, for example.
[0110] Fig. 5 is a view showing a pattern in the form of stripe of the multi-color pattern
sheet of the present embodiment.
[0111] As shown in Fig. 5, on this multi-color pattern sheet 21, patterns 21a, 21b and 21c
in the form of stripe of RGB three colors are formed.
[0112] In Fig. 5, an example of a multi-color pattern sheet having patterns formed in the
form of stripe is exemplified, however, patterns in the form of matrix may also be
formed instead of these pattern in the form of stripe.
[0113] Fig. 6 is a view showing patterns in the form of matrix of the multi-color pattern
sheet of the present embodiment.
[0114] As shown in Fig. 6, on this multi-color pattern sheet 21, patterns 22a, 22b and 22c
in the form of matrix of RGB three colors are formed. For producing the multi-color
pattern sheet having the patterns in the form of matrix, it may be permissible that
a convex portion 23 in the form of matrix is formed on the surface of the pressing
member 30 shown in Fig. 2, and a transfer process is conducted using this pressing
member.
[0115] Next, the application method in the present embodiment will be explained.
[0116] Figs. 7 to 10 are schematic views according to various application modes that can
be adopted in the present embodiment.
[0117] Fig. 7 shows an application method of die coater mode, and ink accommodated in a
die 31 is supplied on a substrate 10 which is carried toward the direction of an arrow
A and ink 32 is applied on the substrate 10.
[0118] Fig. 8 shows an application method of bar coater mode, and ink 32 is applied on a
substrate 10 carried toward the direction of an arrow A, by a bar 34 rotating along
the direction of an arrow B partially immersed in ink in an ink bath 33.
[0119] Fig. 9 shows an application method of gravure coater mode, and ink 32 is applied
on a substrate 10 carried toward the direction of an arrow A, by an application roll
35 immersed in ink in an ink bath 33 and rotating along the direction of an arrow
B and a pressing roll 36 rotating along the direction of an arrow C facing the application
roll 35.
[0120] Fig. 10 shows an application method of spin coater mode, and ink 32 is dropped from
a nozzle 39 on a substrate 10 placed on a rotating table 38 rotation-driven by a motor
37, and the dropped ink spreads on the surface of the substrate 10 by centrifugal
force, to cause ink application on the surface of the substrate 10.
[0121] Next, the multi-color pattern sheet production apparatus of the present invention
will be described.
[0122] Fig. 11 is a schematic constitutional view showing a multi-color pattern sheet production
apparatus which is one embodiment of the pattern member production apparatus of the
present invention.
[0123] As shown in Fig. 11, with this multi-color pattern sheet production apparatus, three
kinds of single color films 11a, 11b and 11c (see Fig. 1) having color ink layers
12a, 12b and 12c of RGB formed on the surface are sequentially overlapped on a transparent
glass substrate 22, and the color ink layers 12a, 12b and 12c on these single color
films 11a, 11b and 11c are sequentially transferred to the transparent glass substrate
22, and this operation is repeated for three colors, to produced a multi-color pattern
sheet (one example of the pattern member referred in the present invention) having
multi-color patterns by three color inks formed on the surface.
[0124] Namely, this multi-color pattern sheet production apparatus comprises transfer means
40 for three colors of transferring the above-mentioned color ink layer of the single
color film to the transparent glass substrate 22, being composed of patterning rolls
41a, 41b and 41c having a convex portion in the form of stripe formed in the surface,
and counter rolls 42a, 42b and 42c placed facing the patterning rolls 41a, 41b and
41c and sandwiching both the transparent glass substrate 22 and any one of the above-mentioned
single color films 11a, 11b and 11c, sheet supplying means 50 for supplying the transparent
glass substrate 22 to the transfer means 40 for R color, and single color film supplying
means 60 for three colors of supplying one single color film of three single color
films 11a, 11b and 11c to between the patterning rolls 41a, 41b and 41c and the transparent
glass substrate 22 supplied to a nip portion 44 sandwiched by the patterning rolls
41a, 41b and 41c and the counter rolls 42a, 42b and 42c, so that the color ink layer
of this single color film is overlapped so as to contact with the transparent glass
substrate 22.
[0125] The single color film supplying means 60 for three colors are composed of a feeding
rolls 61a, 61b and 61c and winding rolls 62a, 62b and 62c.
[0126] The transparent glass substrate 22 in the present embodiment corresponds to the substrate
referred in the present invention, and the substrate is not limited to glass and various
resins and the like can be used.
[0127] Examples of producing a multi-color pattern sheet by this multi-color pattern sheet
production apparatus will be illustrated below.
[0128] Previously, into three kinds of RGB pigments are mixed and dispersed a binder, alcohol
and application aid, respectively, to produce three RGB inks. These three RGB inks
are applied at a width of 1 m and an application speed of 20 m/min on the surface
of a PET (polyethylene terephthalate) film having a thickness of 20µ by a die coater
shown in Fig. 7 and dried, to produced three kinds of single color films 11a, 11b
and 11c (see Fig. 1) having color ink layers 12a, 12b and 12c of RGB three colors
formed on the surface . The application thickness of each color ink is about 20µ in
wet condition and about 0.1µ in dry condition.
[0129] Next, these single color films 11a, 11b and 11c are installed on the single color
film supplying means 60, respectively, composed of the feeding rolls 61a, 61b and
61c and the winding rolls 62a, 62b and 62c of the multi-color pattern sheet production
apparatus shown in Fig. 11.
[0130] Next, the transparent glass substrate 22 is carried toward the direction of an arrow
A by the sheet supplying means 50, and supplied to the nip portion 44 sandwiched by
the patterning roll 41a for R color and the counter roll 42b. To this nip portion
44, the single color film 11a of R color supplied from the feeding roll 61a and wound
by the winding roll 62a is supplied in overlap such that the color ink layer 12a comes
in contact with the transparent glass substrate 22, and parts corresponding to the
pattern of the convex portion 23 of the color ink layer 12a are transferred to the
transparent glass substrate 22 by the patterning roll 41a having a convex portion
of stripe pattern formed on the surface. In this operation, the temperature of each
patterning roll is 150°C, the transfer pressure is 5 kg/cm
2, and the feeding speed of each single color film is 2 m/min.
[0131] Thus, a pattern in the form of stripe having a width of 200µ and an interval of 550µ
is formed on the transparent glass substrate 22. The above-mentioned transfer is conducted
for three RGB single color films, to produce a multi-color pattern sheet continuously.
[0132] Next, the patterning roll used in this multi-color pattern sheet production apparatus
will be described.
[0133] Fig. 12 is a sectional view along the rotation axis direction of the patterning roll
in the present embodiment.
[0134] As shown in Fig. 12, on the surface of the patterning rolls 41a, 41b and 41c (see
Fig. 11), the convex portion 23 of stripe pattern is formed along the peripheral direction,
the positions of the convex portion 23 along the roll width direction of the patterning
rolls mutually differ, and stripes of respective colors are formed at respectively
different positions along the rotation axis direction of the glass substrate 22 (see
Fig. 11).
[0135] The diameter of each patterning roll is 200 mm, and patterning is so conducted that
the width of the convex portion 23 along the roll rotation axis direction is 200 µ,
and the width along the roll rotation axis direction of concave portions other than
the convex portion 23 is 550 µ.
[0136] Each patterning roll contains inside a heat source, and heating is effected by this
heat source and the single color film and the transparent glass substrate are pressed
by this patterning roll and a counter roll situated facing this, to effect transfer
of a color ink layer from the single color films 11a, 11b and 11c to the transparent
glass substrate 22.
[0137] The pattern of the convex portion formed on the patterning roll is not limited to
the pattern in the form of stripe shown in Fig. 12, and the pattern in the form of
matrix as shown in Fig. 6 may also be adopted.
[0138] Other examples will be described below.
[0139] The three RGB inks were changed as shown below, and three single color films 11a,
11b and 11c (see Fig. 1) having color ink layers 12a, 12b and 12c of RGB three colors
formed on the surface of a PET (polyethylene terephthalate) film having a thickness
of 6µ were produced by a die coater shown in Fig. 7. The application thickness of
each color ink was controlled such that it was about 0.05µ under dried condition.
· RGB ink composition:
Compounds selected from the structural formula [chemical formula 1]: 1 part by weight
Structural formula [chemical formula 2] (average molecular weight: 17000): 40 parts
by weight
Dichloroethane: 3200 parts by weight


Regarding the compounds selected from [chemical formula 1], B was selected from B-1
and B-2, G was selected from G-1 and G-2, R was selected from R-1, R-2 and R-3, and
each two kinds of single color films for B and G and three kinds of single color films
for R were produced.
[0140] Though the substrate A described below was used instead of the transparent glass
substrate 22, a multi-color pattern was created likewise.
·Production of substrate A
[0141] A polyimide film (UPILEX-50S, manufactured by UBE INDUSTRIES, LTD.) having a thickness
of 50 µm was charged in a washing vessel, and washed with isopropyl alcohol (IPA),
then, oxygen plasma treatment was conducted. On one surface of a glass plate on which
oxygen plasma treatment had been conducted, Al was deposited in a press-reduced atmosphere
of about 0.1 mPa, to form an electrode having a film thickness of 0.3 µm. Further,
LiF was deposited in the same pattern as for the Al layer, as a dielectric layer,
to obtain a film thickness of 3 nm. An aluminum lead line was connected from the Al
electrode, to form a laminated structure. Next, in a pressure-reduce atmosphere of
about 0.1 mPa, an electron transporting compound having the following structural formula
[chemical formula 3] was deposited, to form an electron transporting organic thin
film layer having a thickness of 9 nm on LiF.

[0142] Then, the following transparent substrate B or C and the substrate A were overlapped
such that the electrodes faced sandwiching a light emitting organic thin film layer,
and they were heated under press and pasted using a couple of heat rollers at 160°C,
0.3 MPa and 0.05 m/min, to obtain excellent RGB pattern color development.
· Production of transparent substrate B
[0143] Using a glass plate having a thickness of 0.5 mm, and this substrate supporting body
was introduced into a vacuum chamber, and using an ITO target having a SnO
2 content of 10 wt% (indium:tin = 95:5 (molar ratio)), a transparent electrode composed
of an ITO thin film having a thickness of 0.2 µm was formed by DC magnetron sputtering
(condition: temperature of substrate supporting body: 250° C, oxygen pressure: 1×10
-3 Pa). The surface resistance of the ITO thin film was 10 Ω/□ . An aluminum lead line
was connected from the transparent electrode (ITO), to form a laminated structure.
The glass plate having the transparent electrode formed thereon was placed in a washing
vessel, and washed with isopropyl alcohol (IPA), then, oxygen plasma treatment was
conducted. On the surface of the treated transparent electrode, an application solution
of the following composition was applied by a die coater shown in Fig. 7, and dried
at room temperature, to form a hole transporting organic thin film layer having a
thickness of 100 nm.
[0144] Hole transporting compound (PTPDES) of the structural formula [chemical formula 4]:
40 parts by weight
Additive (TBPA) of the structural formula [chemical formula 5]: 10 parts by weight
Dichloroethane: 3200 parts

· Production of substrate C
[0145] Production was conducted in the same manner as for the substrate B except that the
solution for producing a hole transporting organic thin film layer was changed to
an aqueous dispersion of polyethylene dioxythiophen polystyrenesulfonic acid (manufactured
by BAYER, Baytron P: solid content: 1.3 wt%) and drying was conducted at 150° C for
2 hours in vacuo.
[0146] The results of BGR pattern light emission are summarized in the following table.
[0147] The uniformity of patterning was observed by a microscope of × 100, and evaluated
as × when deletion is observed, and as ○ when deletion is not observed and uniformity
is excellent.
[0148] In light emission, the light emitting voltage, that is the driving voltage when 100
cd/m
2, was shown in the following table. As a result, it was confirmed that light emission
occurred uniformly by patterning according to the present invention.
[Table 1]
| Selected compound [Chemical formula 1] |
Patterning uniformity |
Light emitting voltage (V) |
Light emitting uniformity |
| Blue color |
Green color |
Red color |
|
B |
G |
R |
|
| B-2 |
G-1 |
R-1 |
○ |
12 |
12 |
16 |
○ |
| B-1 |
G-1 |
R-1 |
○ |
14 |
12 |
16 |
○ |
| B-1 |
G-1 |
R-3 |
○ |
14 |
12 |
18 |
○ |
| B-2 |
G-2 |
R-1 |
○ |
12 |
12 |
16 |
○ |
| B-2 |
G-2 |
R-2 |
○ |
12 |
12 |
16 |
○ |
[0149] As describe above, according to the production method described above, a pattern
member is produced by a single color film production process of producing single color
films of a plurality of colors having a color ink layer formed on the surface, and
a transfer process in which a single color film of one color among the above-mentioned
single color films of a plurality of colors is overlapped on a substrate, and pressed
by a pressing member having a convex portion of given pattern formed on the surface
to transfer the color ink layer to the substrate, and this operation is repeated at
frequency corresponding to a plurality of colors for forming a multi-color pattern
on the subtrate, therefore, a pattern member can be produced with a small number of
processes at low cost.
[0150] A pattern member having a color ink layer of uniform thickness can be produced without
influenced by the physical properties of coloring inks and recipe thereof.
[0151] Further, according to the above-mentioned production apparatus, the equipment cost
is low and an apparatus of producing a pattern member showing high productivity can
be realized since the apparatus comprises transfer means for a plurality of colors
composed of a patterning roll having a convex portion of given pattern formed on the
surface and a counter roll placed facing the patterning roll, substrate supplying
means of supplying a substrate to transfer means for a plurality of colors sequentially,
and single color film supplying means for a plurality of colors of supplying a single
color film of one color to between a patterning roll and a substrate supplied to a
nip portion sandwiched by a patterning roll and a counter roll such that the single
color film is overlapped to the substrate.
[0152] Figs. 13 to 16 are schematic process views showing the first embodiment of the second
method of producing a pattern member of the present invention.
[First Embodiment]
[0153] Three transfer substrates 11 having a thickness of 50 µm as shown in Fig. 13 were
prepared, and a plastic deformation layer 12 is applied on each of the transfer substrates
11. As the transfer material 11, PET (polyethylene terephthalate), PP (polypropylene),
TAC (triacetylcellulose) and the like can be used.
[0154] As the plastic deformation layer 12, layers made of a polymer such as a methacrylic
acid copolymer, crotonic acid copolymer, maleic acid copolymer, itaconic acid copolymer,
partially esterified maleic acid copolymer, polyvinylpyrrolidone, polyethylene oxide,
polyvinyl alcohol, gelatin and the like are listed. Commercially available photo resists
may also be used. For improving film strength, those prepared by adding an alcohol-soluble
nylon or epoxy resin to them may also be used.
[0155] Next, a releasing layer 13 is formed as shown in Fig. 14 on the plastic deformation
layer 12 of these three transfer substrates 11.
[0156] As the releasing layer 13, substances obtained by adding wax such as paraffin wax,
montan-based wax, bisamide-based wax and the like, silicone resins, fluorine-based
compound and the like to the polymer used in the plastic deformation layer 12 are
used. Main polymers in the releasing layer 13 and the plastic deformation layer 12
may be the same or different.
[0157] Next, as shown in Fig. 15, by applying an R ink on the releasing layer 13 on one
transfer material 11 of three transfer materials 11 carrying the releasing layer formed
and drying the ink, a coloring material layer 14R emitting light of Red color is formed
at a thickness of 50 nm when current flows, and a coloring transfer material 15R of
R color is formed (single color transfer material forming process).
[0158] Further, by applying a G ink on the releasing layer 13 on another transfer material
11 and drying the ink, a coloring material layer 14G emitting light of Green color
is formed at a thickness of 50 nm when current flows, and a coloring transfer material
15G of G color is formed (single color transfer material forming process).
[0159] Furthermore, by applying a B ink on the releasing layer 13 on another transfer material
11 and drying the ink, a coloring material layer 14B emitting light of Blue color
is formed at a thickness of 50 nm when current flows, and a coloring transfer material
15B of B color is formed (single color transfer material forming process).
[0160] Next, as shown in Fig. 16, by pressing the surface of the coloring transfer material
15R of R color by a hot press apparatus equipped with a mold 16R (pressing member)
on which a concave portion having a longitudinal length of 200 µm, a transverse length
of 50 µm and a height of 30 µm is arranged regularly in given pattern on the surface
at a temperature of 160° C and a pressure of 800 kg/cm
2 for 5 minutes, the coloring material layer 14R projects by 30 µm on the surface of
the coloring transfer material 15R of R color as shown in Fig. 17 and an irregular
pattern 17R having a depth of 30 µm corresponding to the irregular pattern 17R of
the pressing member (see Fig. 16) is formed.
[0161] Further, pressing is conducted by the pressing member under the same conditions also
for the coloring transfer material 15G of G color and the coloring transfer material
15B of B color, to form given irregular patterns respectively on the surfaces of the
transfer materials (pattern formation process).
[0162] Next, as shown in Fig. 18, the coloring transfer material 15R of R color having the
irregular pattern 18R formed is overlapped on a separately prepared glass substrate
19 having a thickness of 50 µm and allowed to proceed continuously at a speed of 0.05
m/min while being pressed by a rubber roller at a temperature of 160°C and a pressure
of 3 kg/cm
2, to transfer the coloring material layer 14R on the coloring transfer material 15R
of R color to the glass substrate 19. Next, the coloring transfer material 15G of
G color is overlapped on the glass substrate 19 such that the coloring material layer
14G on the coloring transfer material 15G of G color is transferred to a position
adjacent to the coloring material layer 14R on the glass substrate 19, and the coloring
material layer 14G is transferred to the glass substrate 19 under the same conditions
as for the coloring transfer material 15R of R color. Further, the coloring transfer
material 15B of B color is overlapped on the glass substrate 19 such that the coloring
material layer 14B on the coloring transfer material 15B of B color is transferred
to a position adjacent to the coloring material layer 14G on the glass substrate 19,
and the coloring material layer 14B is transferred to the glass substrate 19 under
the same conditions as for the coloring transfer material 15R of R color (transfer
process).
[0163] Thus, as shown in Fig. 19, a pattern member 20 is produced having RGB three color
patterns composed of the coloring material layer 14R, coloring material layer 14G
and coloring material layer 14B formed on the surface of the glass substrate 19.
[0164] In the above-mentioned first embodiment, an example of forming a releasing layer
between a plastic deformation layer and a coloring material layer of each color is
shown, however, the releasing layer can be omitted when its formation is not necessarily
required.
[0165] Likewise, the plastic deformation layer can be omitted when its formation is not
necessarily required.
[0166] In the above-mentioned first embodiment, an example in which formation of a plastic
deformation layer, formation of a releasing layer and formation of a coloring layer
of each color are conducted separately is shown, however, a plastic deformation layer,
releasing layer and a coloring layer of each color may be overlapped and formed simultaneously.
In this case, the conditions shown in Figs. 1 and 2 are not present, and the layer
structure in Fig. 3 is directly formed.
[Second Embodiment]
[0167] Figs. 20 to 23 are schematic process views showing the second embodiment of the second
method of producing a pattern member of the present invention.
[0168] As shown in Fig. 20, an aluminum layer was laminated on a polyimide sheet substrate
having a thickness of 100 µm to produce an oxygen moisture barrier sheet substrate
21. On the opposite surface to the aluminum layers side of the sheet substrate 21,
an Al electrode layer 22 having a thickness of 50 nm is formed by vapor deposition,
further, on this, an electron transporting layer 23 is applied to give a thickness
of 50 nm.
[0169] Next, as shown in Fig. 21, the coloring material layer 14R of the coloring transfer
material 15R of R color having the irregular pattern 18R by the pattern formation
process shown in Fig. 16 is overlapped on the surface of the electron transporting
layer 23 of the sheet substrate 21, and the same transferring process as shown in
Fig. 18 is conducted to transfer the coloring material layer 14R to the sheet substrate
21, further, the transferring process with the coloring transfer material 15G of G
color and the coloring transfer material 15B of B color is repeated on the sheet substrate
21, to transfer the coloring material layer 14G and the coloring material layer 14B,
finally forming an organic EL light emitting layer member 24 of RGB three colors as
shown in Fig. 22.
[0170] Next, as shown in Fig. 23, this organic EL light emitting layer member 24 is pasted
to a member 28 obtained by forming a patterned transparent electrode 26 and hole transporting
layer 27 on a transparent substrate 25, to produce an organic EL display material
29.
[Embodiment 3]
[0171] A coloring material layer having a thickness of 2 µm containing a coloring matter
of R color which causes not light emission is formed, instead of the coloring material
layer 14R emitting light of Red color when current flows in the above-mentioned single
color transfer material forming process of the first embodiment (see Fig. 15), on
the transfer substrate 11 to form a transfer material of R color, and according to
the same manner, a transfer material of G color and a transfer material of B color
are formed.
[0172] Next, the same pattern formation operation and the same transfer operation to a substrate
are conducted as in the pattern formation process and transfer process in the first
embodiment, to produce a patterned color filter.
[0173] As described above, according to the second method of producing the pattern member
of the present invention, treatment can be effected in dry mode, therefore, a material
is not invaded by an etching treatment solution and resist removal solution, and a
pixel pattern of high precision can be formed.
[0174] Since only a coloring material layer of a convex portion is transferred to a substrate
in transfer, transfer can be effected infallibly also on the surface of a substrate
having irregularity on which ITO and the like have been formed.
[0175] Further, since an electron transporting layer, light emitting layer, hole transporting
layer and the like can be laminated in dry mode, interlaminar mixing as in application
of a plurality of layers and printing does not occur, and a pixel pattern can be formed
with high precision and high efficiency.
[0176] Also, since leaking from a mask in vapor deposition does not occur, formation of
fine pixel is possible, a pattern member of high precision can be formed.
[0177] Still further, a single color transfer material formation process, pattern formation
process and transfer process can be conducted continuously, a pattern member can be
produced at low cost.
[0178] According to the pattern member of the present invention, a multi-color pattern member
can be obtained at high productivity and low cost.